Process Validation Engineer- Media Fill

Process Validation Engineer- Media Fill
Location: Greenville, NC
Duration: 6-12 Months

*Background* : The client is a pharmaceutical CDMO looking for a validation engineer to help with media fills.

*Project* : The ideal candidate will have a strong background in validation. The candidate will be expected to have string background in sterile manufacturing processes to ensure compliance with cGMP, FDA, and global regulatory requirements. The ideal candidate will have 5+ years of experience in media fill validation and hands-on expertise in aseptic processing within a sterile manufacturing environment. The responsibilities include developing and reviewing validation protocols, coordinating and executing media fill studies, documenting and analyzing validation results, and performing risk assessments. The role also supports equipment and process qualification, aseptic process simulations, validation lifecycle management. The candidate will be expected to participate in validation activities and make sure things are properly documented, technically sound, inspection-ready, and compliant with regulatory and company quality standards

Benefits: This a contract position does not include employer-provided benefits.

Equal Opportunity Employer:
We are an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to
race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Background Check:
Background checks may be conducted in accordance with applicable law.

Work Authorization:
Applicants must be authorized to work in the United States